HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131890539_131890540insC , CM000668.2:g.131890539_131890540insC | GRCh38 |
NC_000006.11:g.132211679_132211680insC , CM000668.1:g.132211679_132211680insC | GRCh37 |
NC_000006.10:g.132253372_132253373insC | NCBI36 |
NG_008206.1:g.87524_87525insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684674.1:n.1237_1238insC | ||
ENST00000647893.1:c.*28_*29insC MANE Select | ENSP00000498074.1:n.*28_*29insC | |
ENST00000360971.6:c.*28_*29insC | ENSP00000354238.2:n.*28_*29insC | |
ENST00000513998.5:c.*1643_*1644insC | ENSP00000422424.1:n.*1643_*1644insC | |
NM_006208.2:c.*28_*29insC | NP_006199.2:n.*28_*29insC | |
XM_011535896.1:c.*28_*29insC | XP_011534198.1:n.*28_*29insC | |
NM_006208.3:c.*28_*29insC MANE Select | NP_006199.2:n.*28_*29insC |